| ²é¿´: 241 | »Ø¸´: 1 | ||
rootulyssesгæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×Êý¾Ý³ÏÐÄÇóÖú
|
|
¦Ä56.70,61.23,65.35,68.74,71.59,74.87,74.91,77.01,77.85,77.92,80.47,96.32,103.17, 110.84,134.60,154.80,155.94. лл |
» ²ÂÄãϲ»¶
0703µ÷¼Á£¬Ò»Ö¾Ô¸Ìì½ò´óѧ319·Ö
ÒѾÓÐ18È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
334·Ö»úеר˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
±¾¿ÆÖ£ÖÝ´óѧ£¬Ò»Ö¾Ô¸»ª¶«Ê¦·¶´óѧ282Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
305·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ21È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ18È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúһ΢Æ×Êý¾Ý 15 лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ3¸ö»¯ºÏÎïµÄÄ£ºý²éÕÒ£¨¡·80%£©
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú13C΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
rootulysses: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-10-31 17:02:50
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
rootulysses: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-10-31 17:02:50
|
²éѯ½á¹û£º¹²²éµ½331¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3,4,5-Trimethoxyphenyl 1-O-¦Â-apiofuranosyl (1''¡ú6')-¦Â-glucopyranoside C20H30O13 ÏàËÆ¶È:100% Phytochemistry 2002 59 551-556 Iridoid and phenolic glycosides from Morinda coreia Tripetch Kanchanapoom, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,4,5-trimethoxyphenol ¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1995 43 1937-1942 Chemical Evaluation of Betula Species in Japan. I.Constituents of Betula ermanii Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2,4,6-trimethoxyphynol-1-O-¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 1997 28 195-198 Studies on the Chemical Constituents of Thinleaf Adina(Adina rubella)(¢ó) Fan Gaojun and He Zhisheng (Address: He Zhisheng; Shanghai Institute of Materia Medica; Chinese Academy of Sciences; Shanghai); Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,4,5-trimethoxyphenyl-1-O-¦Â-D-apiofuranosyl-(1''¡ú6')-glucopyranoside ÏàËÆ¶È:100% Journal of Chinese Pharmaceutical Sciences 2012 21 88-92 Chemical constituents from Aquilaria sinensis(Lour.) Gilg Dong Chen; Yue-Lin Song; Chun-Xiao Nie; Xu Ma; Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-Hydroxy-3,4,5-trimethoxybenzene-1-O-¦Á-L-apiopyranosyl-(1¡ú 6)-O-¦Â-D-glucopyranoside C20H30O13 ÏàËÆ¶È:94.1% Journal of Asian Natural Products Research 2006 8 571-577 A new meta-homoisoflavane from the fresh stems of dracaena cochinchinensis Q.-A. ZHENG, Y.-J. ZHANG and C.-R. YANG Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3,4,5-trimethoxyphenol ¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyronoside C35H52O20 ÏàËÆ¶È:94.1% Natural Product Research 2009 23 1408-1415 Phenolic and bis-iridoid glycosides from Strychnos cocculoides Fortunatus Sunghwa; Mamoru Koketsu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3,4,5-trimethoxyphenol ¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:89.4% Chemical & Pharmaceutical Bulletin 1997 45 1533-1535 Three New Hemiterpene Glycosides from Ilex macropoda Hiroyuki FUCHINO,Hironori TACHIBANA and Nobutoshi TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (4S)-2,4-dimethyl-3-(3,3-bis-sethoxycarbonylpropyl)-4-methoxycarboxyl-2-cyclohexeo-1-one ÏàËÆ¶È:85% Tetrahedron 1988 44 4703-4711 Structures of potent antiulcerogenic compounds from cinnamomum cassia Yusei Shiraga, Kanemichi Okano, Toshiaki Akira, Chikara Fukaya, Kazumasa Yokoyama, Shigeo Tanaka, Hiroshi Fukui, Mamoru Tabata Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . cinnacassoside C C19H28O13 ÏàËÆ¶È:78.9% Molecules 2013 18 10930-10943 Identification of Compounds from the Water Soluble Extract of Cinnamomum cassia Barks and Their Inhibitory Effects against High-Glucose-Induced Mesangial Cells Qi Luo, Shu-Mei Wang, Qing Lu, Jie Luo and Yong-Xian Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3,5-¶þ¼×Ñõ»ù-4-ôÇ»ù±½·Ó1-O-¦Â-D-ÇÛÌÇ»ù-(1¡ú6)-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:76.4% Chinese Traditional and Herbal Drugs 2008 39 1143-1145 뺼×ÓÉÒ»¯Ñ§³É·ÖµÄÑо¿ ÎÄÆÁ;º«»ÛÓ¢;ÍõÄËÀû;Ò¦ÐÂÉú Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . khaephuoside A C20H30O13 ÏàËÆ¶È:73.6% Phytochemistry 2002 59 565-570 Phenolic glycosides from Barnettia kerrii Tripetch Kanchanapoom, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . canthoside B C19H28O13 ÏàËÆ¶È:72.2% Phytochemistry 2002 61 461-464 Iridoid and phenolic diglycosides from Canthium berberidifolium Tripetch Kanchanapoom, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (2R)-4-(4-hydroxyphenyl)-2-butanol 2-O-¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:72.2% Chemical & Pharmaceutical Bulletin 1995 43 1937-1942 Chemical Evaluation of Betula Species in Japan. I.Constituents of Betula ermanii Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-(¦Á-L-rhamnosyl(1-6)-¦Â-D-glucopyranosyloxy)-3,4,5-trimethoxybenzene ÏàËÆ¶È:72.2% Phytochemistry 1999 52 1145-1148 A phenolic glycoside and N-( p-coumaroyl)-tryptamine from Ravensara anisata Jaconnet O. Andrianaivoravelona, Christian Terreaux, Sevser Sahpaz, Jocelyne Rasolondramanitra, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 1-(¦Á-L-rham(1¡ú6)-¦Â-D-glu)-3,4,5-trimethoxyphenol C21H32O13 ÏàËÆ¶È:72.2% Chinese Journal of Pharmaceuticals 2010 41 823-826 Studies on Chemical Constituents of Celastrus orbiculatus ZHANG Yang, XU Haiyan, TAN Junjie, TAN Changheng, YANG Peiming Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 4-methoxyphenol 1-O-¦Â-D-apiofuranosyl-(1¡ú6)-O-¦Â-Dglucopyranoside C18H26O11 ÏàËÆ¶È:72.2% Natural Product Communications 2011 6 957-960 Phenolic Derivatives from the Leaves of Martinella obovata (Bignoniaceae) Carolina Arevalo*, Ines Ruiz, Anna Lisa Piccinelli, Luca Campone and Luca Rastrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . potalioside B C21H32O14 ÏàËÆ¶È:70.5% Planta Medica 2005 71 977-979 Phenolic Glycosides from Potalia amara Xing-Cong Li , Hala N. ElSohly , Larry A. Walker, Alice M. Clark Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3,4,5-trimetoxyphenil 1-O-¦Â-(6-sulpho)-glucopyranoside C15H22O12S ÏàËÆ¶È:70.5% Phytochemistry 2009 70 641-649 Phenolic compounds from Bursera simaruba Sarg. bark: Phytochemical investigation and quantitative analysis by tandem mass spectrometry Mariateresa Maldini, Paola Montoro, Sonia Piacente, Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-10-30 10:42:01














»Ø¸´´ËÂ¥